Vancová Marie, Rudenko Nataliia, Vaněček Jiří, Golovchenko Maryna, Strnad Martin, Rego Ryan O M, Tichá Lucie, Grubhoffer Libor, Nebesářová Jana
Biology Centre CAS, Institute of ParasitologyČeské Budějovice, Czechia.
Faculty of Science, University of South BohemiaČeské Budějovice, Czechia.
Front Microbiol. 2017 Apr 11;8:596. doi: 10.3389/fmicb.2017.00596. eCollection 2017.
To understand the response of the Lyme disease spirochete exposed to stress conditions and assess the viability of this spirochete, we used a correlative cryo-fluorescence and cryo-scanning microscopy approach. This approach enables simple exposition of bacteria to various experimental conditions that can be stopped at certain time intervals by cryo-immobilization, examination of cell viability without necessity to maintain suitable culture conditions during viability assays, and visualization of structures in their native state at high magnification. We focused on rare and transient events e.g., the formation of round bodies and the presence of membranous blebs in spirochetes exposed to culture medium, host sera either without or with the bacteriolytic effect and water. We described all crucial steps of the workflow, particularly the influence of freeze-etching and accelerating voltage on the visualization of topography. With the help of newly designed cryo-transport device, we achieved greater reproducibility.
为了解莱姆病螺旋体在应激条件下的反应并评估该螺旋体的活力,我们采用了一种相关冷冻荧光和冷冻扫描显微镜方法。这种方法能够使细菌简单地暴露于各种实验条件下,通过冷冻固定可在特定时间间隔停止实验,无需在活力测定期间维持合适的培养条件即可检测细胞活力,并能在高倍放大下观察其天然状态的结构。我们关注了罕见和短暂的事件,例如暴露于培养基、有无溶菌作用的宿主血清以及水的螺旋体中圆形体的形成和膜泡的存在。我们描述了工作流程的所有关键步骤,特别是冷冻蚀刻和加速电压对地形可视化的影响。借助新设计的冷冻运输装置,我们实现了更高的重现性。